Holmium(III) oxide: Difference between revisions

Content deleted Content added
Crystalline structure: replace primary ref with review
m Production: clean up, typo(s) fixed: 3-4 → 3–4
 
(9 intermediate revisions by 6 users not shown)
Line 48:
| GHSPictograms = {{GHS07}}{{GHS09}}
| GHSSignalWord = Warning
| HPhrases = {{H-phrases|319|400|410}}
| PPhrases = {{P-phrases|264|273|280|305+351+338|337+313|391|501}}
 
Line 68:
}}
 
'''Holmium(III) oxide''', or '''holmium oxide''' is a [[chemical compound]] of athe [[rare-earth element]] [[holmium]] and [[oxygen]] with the [[chemical formula|formula]] Ho<sub>2</sub>O<sub>3</sub>. Together with [[dysprosium(III) oxide]] (Dy<sub>2</sub>O<sub>3</sub>), holmium oxide is one of the most powerfully [[Paramagnetism|paramagnetic]] substances known. The oxide, also called '''holmia''', occurs as a component of the related erbium oxide [[mineral]] called [[erbia]]. Typically, the oxides of the trivalent [[lanthanide]]s coexist in nature, and separation of these components requires specialized methods. Holmium oxide is used in making specialty colored [[glass]]es. Glass containing holmium oxide and holmium oxide solutions have a series of sharp [[optical absorption]] peaks in the visible [[spectrum|spectral range]]. They are therefore traditionally used as a convenient calibration standard for [[Monochromator|optical spectrophotometers]].
 
==Properties==
Line 83:
Treating holmium oxide with [[hydrogen chloride]] or with [[ammonium chloride]] affords the corresponding [[holmium(III) chloride|holmium chloride]]:<ref name=patnaik/>
:Ho<sub>2</sub>O<sub>3</sub> + 6 NH<sub>4</sub>Cl → 2 HoCl<sub>3</sub> + 6 NH<sub>3</sub> + 3 H<sub>2</sub>O
 
Holmium(III) oxide can also react with [[hydrogen sulfide]] to form [[holmium(III) sulfide]] at high temperatures.<ref>{{Cite book|editor1=G. Meyer |editor2= Lester R. Morss |title=Synthesis of Lanthanide and Actinide Compounds |publisher=Kluwer Academic Publishers |year=1991 |at=pp.&nbsp;329–335 |isbn=0792310187 |url=https://books.google.com/books?id=bnS5elHL2w8C&pg=PA329|access-date=18 August 2022}}</ref>
 
==History==
Line 99 ⟶ 101:
 
==Occurrence==
[[File:Gadolinitas.jpg|thumb|Gadolinite contains traces of holmium(III) oxide]]Holmium readily oxidizes in air; therefore presence of holmium in nature is synonymous with that of holmia. Holmium oxide occurs in trace amounts in the minerals [[gadolinite]], [[monazite]], and in other rare-earth [[mineral]]s.
[[File:Gadolinitas.jpg|thumb|Gadolinite]]
Holmium oxide occurs in trace amounts in the minerals [[gadolinite]], [[monazite]], and in other rare-earth [[mineral]]s. Holmium metal readily oxidizes in air; therefore presence of holmium in nature is synonymous with that of holmia. With the abundance of 1.4&nbsp;mg/kg, holmium is the 56th most abundant element.<ref name=history/> The main mining areas are [[China]], [[United States]], [[Brazil]], [[India]], [[Sri Lanka]] and [[Australia]] with reserves of holmium oxide estimated as 400,000 tonnes.<ref name=history/>
 
==Production==
A typical extraction process of holmium oxide can be simplified as follows: the mineral mixtures are crushed and ground. Monazite, because of its magnetic properties can be separated by repeated electromagnetic separation. After separation, it is treated with hot concentrated [[sulfuric acid]] to produce water-soluble sulfates of several rare earth elements. The acidic filtrates are partially neutralized with [[sodium hydroxide]] to pH 3-43–4. [[Thorium]] precipitates out of solution as hydroxide and is removed. After that, the solution is treated with [[ammonium oxalate]] to convert rare earths in to their insoluble [[oxalate]]s. The oxalates are converted to oxides by annealing. The oxides are dissolved in [[nitric acid]] that excludes one of the main components, [[cerium]], whose oxide is insoluble in HNO<sub>3</sub>.
 
The most efficient separation routine for holmium oxide from the rare-earths is [[ion exchange]]. In this process, rare-earth ions are adsorbed onto suitable ion-exchange resin by exchange with hydrogen, ammonium or cupric ions present in the resin. The rare earth ions are then selectively washed out by suitable complexing agent, such as ammonium citrate or nitrilotriacetate.<ref name=patnaik>{{cite book|last =Patnaik|first =Pradyot|year = 2003|title =Handbook of Inorganic Chemical Compounds|publisher = McGraw-Hill|pages = 340;445| isbn =0-07-049439-8|url= https://books.google.com/books?id=Xqj-TTzkvTEC&pg=PA445|access-date = 2009-06-06}}</ref>
Line 124 ⟶ 125:
[[Category:Holmium compounds]]
[[Category:Sesquioxides]]
[[Category:Crystals in space group 206]]